No more wires: new system could make prosthetic hands easier to use
NCT ID NCT06821412
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This completed study tested a new wireless electrode system, called ASTERISK, for controlling prosthetic hands in people with below-elbow amputations. Four current prosthetic hand users tried both the wireless system and a standard wired setup for one month each. The goal was to see if the wireless system improved comfort and satisfaction.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ASTERISK System (wireless EMG electrode device)
- What this could lead to
- If successful, this wireless system could make prosthetic hands more comfortable and easier to control, removing the need for wires.
- What could go wrong
- This was a very small, early-stage trial with only 4 participants. The results may not apply to everyone, and the device is not yet available commercially.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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4 people
The number who actually took part.
- Started
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Jun 2024
- Finished
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Jun 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 89 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * current wearers of trans-radial myoelectric prostheses or orthoses * have used their prostheses/orthoses for at least six months * understand spoken and written English (for the purpose of consenting) Exclusion Criteria: * have any neurological or physical conditions which would prevent them from performing the experimental tasks * are pregnant
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Liberating Technologies, Inc.
Holliston, Massachusetts, 01746, United States
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